marine drugs
ArticleComparative Evaluation of Different Chitosan Species and
Derivatives as Candidate Biomaterials for Oxygen-Loaded
Nanodroplet Formulations to Treat Chronic Wounds
Monica Argenziano1 , Bruno Bressan2,3, Anna Luganini4 , Nicole Finesso3, Tullio Genova5 , Adriano Troia6, Giuliana Giribaldi3 , Giuliana Banche7 , Narcisa Mandras7 , Anna Maria Cuffini7, Roberta Cavalli1,*,†and Mauro Prato2,7,*,†
Citation: Argenziano, M.; Bressan, B.; Luganini, A.; Finesso, N.; Genova, T.; Troia, A.; Giribaldi, G.; Banche, G.; Mandras, N.; Cuffini, A.M.; et al. Comparative Evaluation of Different Chitosan Species and Derivatives as Candidate Biomaterials for Oxygen-Loaded Nanodroplet Formulations to Treat Chronic Wounds. Mar. Drugs 2021, 19, 112. https://doi.org/10.3390/md19020112
Academic Editor: Juan Rubio Received: 15 January 2021 Accepted: 11 February 2021 Published: 15 February 2021
Publisher’s Note: MDPI stays neu-tral with regard to jurisdictional clai-ms in published maps and institutio-nal affiliations.
Copyright:© 2021 by the authors. Li-censee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and con-ditions of the Creative Commons At-tribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).
1 Department of Drug Science and Technology, University of Turin, 10125 Turin, Italy;
monica.argenziano@unito.it
2 Department of Neuroscience, University of Turin, 10126 Turin, Italy; brexanb@gmail.com 3 Department of Oncology, University of Turin, 10126 Turin, Italy; nicole.finesso@unito.it (N.F.);
giuliana.giribaldi@unito.it (G.G.)
4 Department of Life Sciences and Systems Biology, University of Turin, 10123 Turin, Italy;
anna.luganini@unito.it
5 Department of Surgical Sciences, University of Turin, 10126 Turin, Italy; tullio.genova@unito.it 6 Istituto Nazionale di Ricerca Metrologica (INRIM), 10135 Torino, Italy; a.troia@inrim.it 7 Department of Public Health and Pediatric Sciences, University of Turin, 10126 Turin, Italy;
giuliana.banche@unito.it (G.B.); narcisa.mandras@unito.it (N.M.); annamaria.cuffini@unito.it (A.M.C.)
* Correspondence: roberta.cavalli@unito.it (R.C.); mauro.prato@unito.it (M.P.); Tel.: +39-011-670-7190 (R.C.); +39-011-670-5843 (M.P.); Fax: +39-011-670-7687 (R.C.); +39-011-670-5845 (M.P.)
† These authors contributed equally to this work.
Abstract: Persistent hypoxia is a main clinical feature of chronic wounds. Intriguingly, oxygen-loaded nanodroplets (OLNDs), filled with oxygen-solving 2H,3H-decafluoropentane and shelled with polysaccharides, have been proposed as a promising tool to counteract hypoxia by releasing a clinically relevant oxygen amount in a time-sustained manner. Here, four different types of chitosan (low or medium weight (LW or MW), glycol-(G-), and methylglycol-(MG-) chitosan) were compared as candidate biopolymers for shell manufacturing. The aim of the work was to design OLND formulations with optimized physico-chemical characteristics, efficacy in oxygen release, and biocompatibility. All OLND formulations displayed spherical morphology, cationic surfaces,
≤500 nm diameters (with LW chitosan-shelled OLNDs being the smallest), high stability, good oxygen encapsulation efficiency, and prolonged oxygen release kinetics. Upon cellular internalization, LW, MW, and G-chitosan-shelled nanodroplets did not significantly affect the viability, health, or metabolic activity of human keratinocytes (HaCaT cell line). On the contrary, MG-chitosan-shelled nanodroplets showed very poor biocompatibility. Combining the physico-chemical and the biological results obtained, LW chitosan emerges as the best candidate biopolymer for future OLND application as a skin device to treat chronic wounds.
Keywords:nanodroplets; oxygen; chitosan; chitosan-derivatives; chronic wound; human keratinocytes
1. Introduction
Chronic wounds, including bedsores, burns, and diabetes-associated vasculopathies, are commonly defined as nonhealing breaks in the epithelial continuity of the skin lasting for more than 42 days [1]. Notably, chronic wounds have become in the last decades an alarming emergency, affecting a large fraction of the population worldwide and the elderly especially, with 1–2% of the population of developed countries being estimated to experience at least one chronic wound during a lifetime [2]. Therefore, the search and the development of new cost-effective treatments that might allow a significant percentage
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of chronic wounds to heal quickly and definitively appears extremely urgent, as it would substantially affect the global healthcare system [3].
From a physio-pathological perspective, these nonhealing lacerations are generally characterized by persistent hypoxia, exacerbated inflammation, and unbalanced levels between proteinases and their inhibitors, which are essential to accomplish the re-modeling phase of healing [4–6]. In addition, microbial infection can represent a recurrent severe complication [7]. In particular, the management of extreme hypoxia in chronic wounds represents a major limit to overcome, and oxygen supply and tension in the wound bed are both crucial issues that need to be addressed in order to promote physiological wound healing. A minimum tissue oxygen tension of 20 mmHg is required for a wound to heal; however, oxygen tension runs at around 5 mmHg in nonhealing wounds [8,9]. Notably, when the arterial blood cannot supply cells with relevant amounts of oxygen, the risks for inflammation, infection, and scarring in wounds are enhanced, since responses to hypoxia are virtually involved in all wound healing and re-modeling processes, including collagen deposition, epithelialization, fibroplasia, angiogenesis, and resistance to infections [8,9]. Another important issue revolves around medical therapy, as the effectiveness of treatments often decreases while tissue necrosis can develop in hypoxic conditions [9]. Oxygen tissue levels can be adequately bolstered by hyperbaric oxygen therapy (HBOT) [10], while an alternative therapy is represented by topical oxygen therapy (TOT) [11]. Unfortunately, either HBOT or TOT display various backwards. On the one hand, the HBOT approach is relatively expensive, uneasy, and even dangerous due to fire accident risks [12]. Ad-ditionally, it may cause severe side effects, including myopia, brain toxicity associated with seizures, and pneumothorax [13]. On the other hand, TOT—which is cheaper and associates with lower toxicity—often fails to effectively trespass the stratum corneum of the skin and to deliver oxygen adequately to fibroblasts, keratinocytes, and inflammatory cells for restoring their functions [12]. For these reasons, intensive research has been focused in the recent years on the development of new oxygen carriers, including hemoglobin-based carriers and perfluorocarbon-containing formulations [14]. Among perfluorocarbon emul-sions of the first generation, Fluosol®is the only medical device approved by the Food and Drugs Administration and unfortunately no perfluorocarbon-based oxygen emulsion of the second generation is currently approved for clinical uses [15].
In this context, nanomedicine has become a major area of interest for oxygen delivery due to its many unique characteristics [16–19]. Interestingly, the physico-chemical prop-erties of nanocarriers, including their high surface-to-volume ratio, small size, stability, and controlled drug release enhance their chances to trespass barriers such as the skin and to reach the biological target [20]. In addition, several nanocarriers can be endowed with an inherent antimicrobial activity, thus synergizing with the antimicrobial efficacy of a coupled antibiotic [21]. All these findings appear extremely intriguing, since they may be exploited to produce innovative and nonconventional nanotherapies for wound management [22,23].
In particular, over the last decade our collaborating interdisciplinary research network has been working to develop new platforms of oxygen carriers to be employed either for diagnostic or for therapeutic purposes, leading to the production of so-called oxygen-loaded microbubbles (OLMBs) [24], nanobubbles (OLNBs) [25,26], and nanodroplets (OL-NDs) [27–31]. Structurally, these carriers display a typical core/shell architecture. For the manufacturing of the outer shell, several alternative polysaccharides (chitosan or dextran usually) can be employed, whereas specific oxygen-solving fluorocarbons (perfluoropen-tane (PFP) for OLMBs or OLNBs, and 2H,3H-decafluoropen(perfluoropen-tane (DFP) for OLNDs) have been selected for the inner core.
Among all three platforms, to date OLNDs are likely to represent the more effective oxygen-releasing carrier to be potentially employed for the treatment of hypoxia-related pathologies. Indeed, the DFP peculiar structure allows oxygen molecules to solubilize not only through van der Waals forces, as for PFP, but also by establishing hydrogen intermolecular bonds [32]. As a consequence, DFP incorporates biatomic oxygen more effectively than PFP while its release by diffusion appears slower and sustained over
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time [27,28]. Nevertheless, nanodroplets still conserve all the peculiar characteristics of nanobubbles, including nanometric size, surface charge, stability, biocompatibility, and re-sponsiveness to ultrasounds (US) [27,28]. The latter property appears crucial, since it allows the nanocarriers to trespass biological barriers through sonophoresis [33]. Interestingly, US irradiation was reported to induce DFP vaporization [34], thus promoting the transfor-mation of nanodroplets into nanobubbles and allowing them to undergo cavitation and sonophoresis. This is consistent with either in vitro or in vivo data showing US-dependent effective trespassing of skin layers by nanodroplets [27,28,35,36] along with higher and more time-sustained oxygen release from oxygen-loaded nanodroplets (OLNDs) with respect to oxygen-free nanodroplets (OFNDs) [27,28]. Due to all these properties, chitosan OLNDs have been proposed as potential therapeutic tools to treat hypoxia-associated pathologies, including chronic wounds, preeclampsia, and cancer. In this context, a se-ries of studies were conducted to investigate the effects of hypoxia and OLNDs on the regulation of cellular secretion of inflammation- and matrix degradation-related soluble factors. Encouragingly, chitosan OLNDs proved to be able to abrogate the dysregulating effects induced by hypoxia, promoting a normoxia-like phenotype in all the hypoxic cells or tissues under investigation [37,38]. Moreover, chitosan-shelled OLND have been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Candida albicans infections—two recurring complicating agents in chronic wounds—due to chitosan natural antimicrobial properties [35].
To further optimize chitosan OLND effectiveness for the potential treatment of chronic wounds, in the present work we aimed at investigating different types of chitosan as a candidate biopolymer to be used as OLND shell’s component. A series of chitosan OLNDs such as low weight (LW), medium weight (MW), glycol-(G-), or methylglycol-(MG-) chitosan-shelled OLNDs were prepared and in vitro characterized comparing their physico-chemical properties, efficacy in oxygen releasing, and biocompatibility with human skin cells.
2. Results
2.1. Characterisation of Chitosan-Shelled ND Formulations
ND formulations were prepared by employing different types of chitosan, such as LW, MW, G-, and MG-chitosan. Figure1showed the chemical structure of the different types of chitosan used.
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pathologies. Indeed, the DFP peculiar structure allows oxygen molecules to solubilize not only through van der Waals forces, as for PFP, but also by establishing hydrogen inter-molecular bonds [32]. As a consequence, DFP incorporates biatomic oxygen more effec-tively than PFP while its release by diffusion appears slower and sustained over time [27,28]. Nevertheless, nanodroplets still conserve all the peculiar characteristics of nano-bubbles, including nanometric size, surface charge, stability, biocompatibility, and re-sponsiveness to ultrasounds (US) [27,28]. The latter property appears crucial, since it al-lows the nanocarriers to trespass biological barriers through sonophoresis [33]. Interest-ingly, US irradiation was reported to induce DFP vaporization [34], thus promoting the transformation of nanodroplets into nanobubbles and allowing them to undergo cavita-tion and sonophoresis. This is consistent with either in vitro or in vivo data showing US-dependent effective trespassing of skin layers by nanodroplets [27,28,35,36] along with higher and more time-sustained oxygen release from oxygen-loaded nanodroplets (OLNDs) with respect to oxygen-free nanodroplets (OFNDs) [27,28]. Due to all these properties, chitosan OLNDs have been proposed as potential therapeutic tools to treat hypoxia-associated pathologies, including chronic wounds, preeclampsia, and cancer. In this context, a series of studies were conducted to investigate the effects of hypoxia and OLNDs on the regulation of cellular secretion of inflammation- and matrix degradation-related soluble factors. Encouragingly, chitosan OLNDs proved to be able to abrogate the dysregulating effects induced by hypoxia, promoting a normoxia-like phenotype in all the hypoxic cells or tissues under investigation [37,38]. Moreover, chitosan-shelled OLND have been shown to be effective against methicillin-resistant Staphylococcus aureus (MRSA) and Candida albicans infections―two recurring complicating agents in chronic wounds―due to chitosan natural antimicrobial properties [35].
To further optimize chitosan OLND effectiveness for the potential treatment of chronic wounds, in the present work we aimed at investigating different types of chitosan as a candidate biopolymer to be used as OLND shell’s component. A series of chitosan OLNDs such as low weight (LW), medium weight (MW), glycol-(G-), or methylglycol-(MG-) chitosan-shelled OLNDs were prepared and in vitro characterized comparing their physico-chemical properties, efficacy in oxygen releasing, and biocompatibility with hu-man skin cells.
2. Results
2.1. Characterisation of Chitosan-Shelled ND Formulations
ND formulations were prepared by employing different types of chitosan, such as LW, MW, G-, and MG-chitosan. Figure 1 showed the chemical structure of the different types of chitosan used.
Figure 1. Chemical structure of chitosan (low weight (LW-), medium weight (MW-c)), glycol chitosan (GC-c), methylglycol chitosan (MG-c).
After manufacturing, chitosan-coated oxygen-loaded nanodroplet (cOLND) formu-lations were characterized physico-chemically by TEM, and dynamic light scattering anal-yses. The physico-chemical characteristics of cOLNDs are reported in Table 1.
Figure 1.Chemical structure of chitosan (low weight (LW-), medium weight (MW-c)), glycol chitosan (GC-c), methylglycol chitosan (MG-c).
After manufacturing, chitosan-coated oxygen-loaded nanodroplet (cOLND) formula-tions were characterized physico-chemically by TEM, and dynamic light scattering analyses. The physico-chemical characteristics of cOLNDs are reported in Table1.
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Table 1.Physico-chemical characterization of chitosan-coated oxygen-loaded nanodroplets (cOLNDs). LW, MW, G-, and MG-cOLNDs were characterized for average diameter, polydispersity index, and zeta potential by dynamic light scattering. Osmolarity and viscosity were measured using an osmometer and an Ubbelohde capillary viscosimeter, respectively. Results are shown as mean±SD from ten preparations. See also Figure1for further details on nanodroplet structure and morphology.
Chitosan Average Diameter (nm±SD) Polydispersity Index±SD Zeta Potential (mV±SD) Osmolarity (mOsm±SD) Viscosity (cP±SD) LW 418.2±22.3 0.20±0.02 +32.4±3.5 282±0.6 1.32±0.01 MW 502.1±16.8 0.19±0.01 +30.2±2.8 284±0.5 1.38±0.02 G- 437.2±23.7 0.22±0.01 +22.9±5.4 285±0.4 1.35±0.02 MG- 456.4±27.4 0.24±0.02 +40.5±3.7 290±0.8 1.34±0.02
Figure2shows representative images of cOLND morphology.
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Table 1. Physico-chemical characterization of chitosan-coated oxygen-loaded nanodroplets (cOLNDs). LW, MW, G-, and MG-cOLNDs were characterized for average diameter, polydispersity index, and zeta potential by dynamic light scatter-ing. Osmolarity and viscosity were measured using an osmometer and an Ubbelohde capillary viscosimeter, respectively. Results are shown as mean ± SD from ten preparations. See also Figure 1 for further details on nanodroplet structure and morphology.
Chitosan Average Diameter (nm ± SD) Polydispersity Index ± SD Zeta Potential (mV ± SD) Osmolarity (mOsm ± SD) Viscosity (cP ± SD) LW 418.2 ± 22.3 0.20 ± 0.02 +32.4 ± 3.5 282 ± 0.6 1.32 ± 0.01 MW 502.1 ± 16.8 0.19 ± 0.01 +30.2 ± 2.8 284 ± 0.5 1.38 ± 0.02 G- 437.2 ± 23.7 0.22 ± 0.01 +22.9 ± 5.4 285 ± 0.4 1.35 ± 0.02 MG- 456.4 ± 27.4 0.24 ± 0.02 +40.5 ± 3.7 290 ± 0.8 1.34 ± 0.02
Figure 2 shows representative images of cOLND morphology.
Figure 2. TEM images displaying chitosan-shelled oxygen-loaded nanodroplets (OLND) spherical morphology and shell-core structure. LW and MW cOLNDs were comparatively analyzed by TEM. Results are shown as representative images from ten different preparations. (A) LW cOLNDs. (B) MW cOLNDs. Magnification: 28,500×.
All OLNDs displayed spherical shapes with a core-shell structure, as emerged from TEM analyses. All sizes were in the nanometer range (~400–500 nm as average diameters), with LW cOLNDs being the smallest and MW cOLNDs the largest. All polydispersity indexes were included between 0.19 and 0.24. Zeta potentials ranged from +22.9 (G-cOLNDs) to +40.5 mV (MG-(G-cOLNDs). Oxygen content was similar in all cOLND formu-lations (~45 mg/L). Figure 3 shows the FTIR spectra of the four chitosan-shelled OLND formulations compared to free chitosan and non-shelled OLNDs. As a control the spec-trum of dipalmitoylphosphatidylcholine (DPPC) was also reported.
Figure 2.TEM images displaying chitosan-shelled oxygen-loaded nanodroplets (OLND) spherical morphology and shell-core structure. LW and MW cOLNDs were comparatively analyzed by TEM. Results are shown as representative images from ten different preparations. (A) LW cOLNDs. (B) MW cOLNDs. Magnification: 28,500×.
All OLNDs displayed spherical shapes with a core-shell structure, as emerged from TEM analyses. All sizes were in the nanometer range (~400–500 nm as average diameters), with LW cOLNDs being the smallest and MW cOLNDs the largest. All polydispersity in-dexes were included between 0.19 and 0.24. Zeta potentials ranged from +22.9 (G-cOLNDs) to +40.5 mV (MG-cOLNDs). Oxygen content was similar in all cOLND formulations (~45 mg/L). Figure3shows the FTIR spectra of the four chitosan-shelled OLND formu-lations compared to free chitosan and non-shelled OLNDs. As a control the spectrum of dipalmitoylphosphatidylcholine (DPPC) was also reported.
The characteristic peaks of DPPC at 2857 and 2919 cm−1 corresponding to CH2 symmetric and asymmetric stretching vibrations, respectively, and at 1735 cm−1attributed to C = O stretching were clearly detected in the spectrum of non-shelled OLNDs, indicating the presence of the phospholipids on the outer surface of the nanostructure. On the contrary, a shift or disappearance of DPPC peaks were observed for shelled ND formulations, indicating the strong interaction of chitosan with the phospholipid monolayer. Moreover, peak modifications at 1589 cm−1corresponding to the N–H bending of the primary amine were observed among free chitosan and chitosan-shelled OLNDs.
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Figure 3. FTIR spectra of chitosan-shelled OLND formulations compared to free chitosan, non-shelled OLNDs, and dipal-mitoylphosphatidylcholine (DPPC).
The characteristic peaks of DPPC at 2857 and 2919 cm–1 corresponding to CH2 sym-metric and asymsym-metric stretching vibrations, respectively, and at 1735 cm–1 attributed to C = O stretching were clearly detected in the spectrum of non-shelled OLNDs, indicating the presence of the phospholipids on the outer surface of the nanostructure. On the con-trary, a shift or disappearance of DPPC peaks were observed for shelled ND formulations, indicating the strong interaction of chitosan with the phospholipid monolayer. Moreover, peak modifications at 1589 cm–1 corresponding to the N–H bending of the primary amine were observed among free chitosan and chitosan-shelled OLNDs.
OLND formulations proved to be physically stable over time, as confirmed by long-term checking of their physico-chemical parameters. Indeed, the obtained values did not remarkably change up to six months after the manufacturing of the formulations stored at 4 °C (data not shown). The mucoadhesive properties of cOLND formulations were eval-uated by in vitro mucin adhesion assay. The percentage of mucin adhesive to cOLNDs was higher than 80% for all the cOLND formulations, indicating the interaction between cOLNDs and the mucin. The presence of oxygen did not affect cOLND mucoadhesive properties, indeed similar results were obtained with chitosan-coated oxygen-free nanodroplet (cOFND) formulations.
2.2. In Vitro Oxygen Release from cOLND Formulations
LW, MW, G-, and MG- cOLND as well as oxygen solution (OSS) abilities to release oxygen in vitro were comparatively evaluated by oximetry. Results are shown in Figure 4.
Figure 3. FTIR spectra of chitosan-shelled OLND formulations compared to free chitosan, non-shelled OLNDs, and di-palmitoylphosphatidylcholine (DPPC). (A) FTIR spectra of LW chitosan, LW cOLNDs, non-shelled OLNDs, and DPPC; (B) FTIR spectra of MW chitosan, MW cOLNDs, non-shelled OLNDs, and DPPC; (C) FTIR spectra of G-chitosan, G-cOLNDs, non-shelled OLNDs, and DPPC; (D) FTIR spectra of MG-chitosan, MG-cOLNDs, non-shelled OLNDs, and DPPC.
OLND formulations proved to be physically stable over time, as confirmed by long-term checking of their physico-chemical parameters. Indeed, the obtained values did not remarkably change up to six months after the manufacturing of the formulations stored at 4◦C (data not shown). The mucoadhesive properties of cOLND formulations were evaluated by in vitro mucin adhesion assay. The percentage of mucin adhesive to cOLNDs was higher than 80% for all the cOLND formulations, indicating the interaction between cOLNDs and the mucin. The presence of oxygen did not affect cOLND mucoadhesive prop-erties, indeed similar results were obtained with chitosan-coated oxygen-free nanodroplet (cOFND) formulations.
2.2. In Vitro Oxygen Release from cOLND Formulations
LW, MW, G-, and MG- cOLND as well as oxygen solution (OSS) abilities to release oxygen in vitro were comparatively evaluated by oximetry. Results are shown in Figure4.
When the nanoformulations were immersed in the hypoxic solution, a prolonged oxygen release profile up to 24 h for all the cOLNDs was observed. There were no significant differences among all four cOLND formulations, proving that they were able to release oxygen through a passive diffusion mechanism, independently from the polysaccharide chosen for the shell. On the contrary, oxygen coming from OSS diffused rapidly in the hypoxic solution, being immediately available, but it led to a great dip-off quite early.
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Figure 4. In vitro oxygen release from chitosan-shelled OLNDs and oxygen solution (OSS). LW, MW, G-, and MG-cOLND
nanosuspensions as well as OSS were comparatively monitored up to 24 h through an oximeter for oxygen release by diffusion in a hypoxic phase. Results are shown as means ± SD from three independent experiments.
When the nanoformulations were immersed in the hypoxic solution, a prolonged
ox-ygen release profile up to 24 h for all the cOLNDs was observed. There were no significant
differences among all four cOLND formulations, proving that they were able to release
oxygen through a passive diffusion mechanism, independently from the polysaccharide
chosen for the shell. On the contrary, oxygen coming from OSS diffused rapidly in the
hypoxic solution, being immediately available, but it led to a great dip-off quite early.
2.3. ND Internalisation by Human Keratinocytes
The mechanical interaction between MW, LW, G-, and MG-cOLNDs or cOFNDs and
human keratinocytes was investigated through analysis by confocal microscopy. As
shown in Figure 5, all ND formulations were avidly internalized into the cytoplasm of
human keratinocytes after 24 h of incubation, independently from the type of
polysaccha-ride chosen for the shell and from the presence or absence of oxygen within the core.
Figure 5. ND internalization by human keratinocytes. Human keratinocyte (HaCaT) cells were left untreated or treated
with 10% v/v 6-coumarin-labeled MW, LW, G-, or MG-chitosan shelled OLNDs (left panels) or oxygen-free nanodroplets (OFNDs) (right panels) for 24 h. After PI staining, cells were checked by confocal microscopy. Results are shown as repre-sentative images from three independent experiments. Red: HaCaT cell nuclei after PI staining. Green: 6-coumarin-labeled NDs. Magnification: 60×.
Figure 4. In vitro oxygen release from chitosan-shelled OLNDs and oxygen solution (OSS). LW, MW, G-, and MG-cOLND nanosuspensions as well as OSS were comparatively monitored up to 24 h through an oximeter for oxygen release by diffusion in a hypoxic phase. Results are shown as means±SD from three independent experiments.
2.3. ND Internalisation by Human Keratinocytes
The mechanical interaction between MW, LW, G-, and MG-cOLNDs or cOFNDs and human keratinocytes was investigated through analysis by confocal microscopy. As shown in Figure5, all ND formulations were avidly internalized into the cytoplasm of human keratinocytes after 24 h of incubation, independently from the type of polysaccharide chosen for the shell and from the presence or absence of oxygen within the core.
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Figure 4. In vitro oxygen release from chitosan-shelled OLNDs and oxygen solution (OSS). LW, MW, G-, and MG-cOLND nanosuspensions as well as OSS were comparatively monitored up to 24 h through an oximeter for oxygen release by diffusion in a hypoxic phase. Results are shown as means ± SD from three independent experiments.
When the nanoformulations were immersed in the hypoxic solution, a prolonged ox-ygen release profile up to 24 h for all the cOLNDs was observed. There were no significant differences among all four cOLND formulations, proving that they were able to release oxygen through a passive diffusion mechanism, independently from the polysaccharide chosen for the shell. On the contrary, oxygen coming from OSS diffused rapidly in the hypoxic solution, being immediately available, but it led to a great dip-off quite early. 2.3. ND Internalisation by Human Keratinocytes
The mechanical interaction between MW, LW, G-, and MG-cOLNDs or cOFNDs and human keratinocytes was investigated through analysis by confocal microscopy. As shown in Figure 5, all ND formulations were avidly internalized into the cytoplasm of human keratinocytes after 24 h of incubation, independently from the type of polysaccha-ride chosen for the shell and from the presence or absence of oxygen within the core.
Figure 5. ND internalization by human keratinocytes. Human keratinocyte (HaCaT) cells were left untreated or treated with 10% v/v 6-coumarin-labeled MW, LW, G-, or MG-chitosan shelled OLNDs (left panels) or oxygen-free nanodroplets (OFNDs) (right panels) for 24 h. After PI staining, cells were checked by confocal microscopy. Results are shown as repre-sentative images from three independent experiments. Red: HaCaT cell nuclei after PI staining. Green: 6-coumarin-labeled NDs. Magnification: 60×.
Figure 5.ND internalization by human keratinocytes. Human keratinocyte (HaCaT) cells were left untreated or treated with 10% v/v 6-coumarin-labeled MW, LW, G-, or MG-chitosan shelled OLNDs (left panels) or oxygen-free nanodroplets (OFNDs) (right panels) for 24 h. After PI staining, cells were checked by confocal microscopy. Results are shown as representative images from three independent experiments. Red: HaCaT cell nuclei after PI staining. Green: 6-coumarin-labeled NDs. Magnification: 60×.
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2.4. Chitosan and ND Biocompatibility with Human Keratinocytes
The biocompatibility of MW, LW, G-, and MG-cOLNDs or cOFNDs as well as free chitosan solutions with human keratinocytes was evaluated over time up to 24 h by using a series of complementary biochemical assays. Specifically, cell viability was checked by MTT assay, treatment cytotoxicity was analyzed by LDH assay, and cell metabolic activity was measured by ATP assay. As shown in Figure6(A: MTT; B: LDH; and C: ATP assays, respectively), all the treatments containing MW, LW, or G-chitosan appeared to be highly compatible with viability, health, and metabolism of human keratinocytes.
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2.4. Chitosan and ND Biocompatibility with Human Keratinocytes
The biocompatibility of MW, LW, G-, and MG-cOLNDs or cOFNDs as well as free
chitosan solutions with human keratinocytes was evaluated over time up to 24 h by using
a series of complementary biochemical assays. Specifically, cell viability was checked by
MTT assay, treatment cytotoxicity was analyzed by LDH assay, and cell metabolic activity
was measured by ATP assay. As shown in Figure 6 (A: MTT; B: LDH; and C: ATP assays,
respectively), all the treatments containing MW, LW, or G-chitosan appeared to be highly
compatible with viability, health, and metabolism of human keratinocytes.
Figure 6. Biocompatibility of chitosan-shelled OLNDs or oxygen-free nanodroplets (OFNDs) with human keratinocytes
in vitro. HaCaT cells were left untreated or treated with 10% v/v MW, LW, G-, or MG-chitosan free solution, cOLNDs or cOFNDs for 24 h. Thereafter, cell viability (A), treatment cytotoxicity (B), and cell metabolic activity (C) were measured through MTT, LDH, and ATP assays, respectively. Results are shown as means ± SEM from three independent experi-ments. Data were also evaluated for significance by ANOVA. (A) Versus untreated cells: * p < 0.05; ** p < 0.005; *** p < 0.0005; **** p < 0.0001. (B) Versus untreated cells: * p < 0.02; ** p < 0.01; **** p < 0.0001. Versus cells treated with free chitosan solution: °°° p < 0.001. (C) Versus untreated cells: ** p < 0.01; **** p < 0.0001. Versus cells treated with free chitosan solution: °°° p < 0.0005. Versus cells treated with cOLNDs: # p < 0.05.
On the contrary, the treatments containing MG-chitosan appeared to be highly toxic
to cells. Interestingly, for each chitosan species or derivative considered, no significant
differences in biocompatibility were highlighted between ND formulations (either with
or without oxygen in the core) and the free solution counterpart.
3. Discussion
Figure 6.Biocompatibility of chitosan-shelled OLNDs or oxygen-free nanodroplets (OFNDs) with human keratinocytes in vitro. HaCaT cells were left untreated or treated with 10% v/v MW, LW, G-, or MG-chitosan free solution, cOLNDs or cOFNDs for 24 h. Thereafter, cell viability (A), treatment cytotoxicity (B), and cell metabolic activity (C) were measured through MTT, LDH, and ATP assays, respectively. Results are shown as means±SEM from three independent experiments. Data were also evaluated for significance by ANOVA. (A) Versus untreated cells: * p < 0.05; ** p < 0.005; *** p < 0.0005; **** p < 0.0001. (B) Versus untreated cells: * p < 0.02; ** p < 0.01; **** p < 0.0001. Versus cells treated with free chitosan solution:◦◦◦p < 0.001. (C) Versus untreated cells: ** p < 0.01; **** p < 0.0001. Versus cells treated with free chitosan solution:◦◦◦p < 0.0005. Versus cells treated with cOLNDs: # p < 0.05.
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On the contrary, the treatments containing MG-chitosan appeared to be highly toxic to cells. Interestingly, for each chitosan species or derivative considered, no significant differences in biocompatibility were highlighted between ND formulations (either with or without oxygen in the core) and the free solution counterpart.
3. Discussion
Chitin and chitosan have emerged as promising polysaccharides to be employed as can-didate biomaterials for the development of new nanomedical devices [39,40]. Chitin, a long-chain polymer composed of repeated units of β-D-(acetylamino)-2deoxy-glucopyranose (N-acetyl-D-glucosamine), represents the second ubiquitous natural polysaccharide on Earth after cellulose. This very common polysaccharide can be found either in the exoskele-ton or the internal structures of various invertebrates, such as crustaceans and insects [41]. Upon N-deacetylation of chitin, chitosan is generated. However, it should be noted that “chitosan” is quite a collective term, as it sums up together a wide spectrum of linear polysaccharides with different molecular weight, viscosity, and degree of deacetylation (ranging from 40% to 98%) [42]. Generally speaking, chitosan can be defined as an amino-polysaccharide composed of randomly distributed β-(1→4)-linked units of deacetylated and acetylated chitin (D-glucosamine and N-acetyl-D-glucosamine, respectively). This natu-rally abundant and renewable cationic polysaccharide displays excellent physico-chemical and biological properties, which are strongly influenced by its molecular weight and degree of deacetylation [43]. Chitosan stands out for its strongly basic nature, due to the proto-natable amino groups present in the polymer chains [41]. The protonation constant (pKa) of chitosan is of about 6, depending on its molecular weight and degree of deacetylation. For this reason, it is soluble in acidic aqueous solutions [44]. The number of N-acetyl groups in chitosan strongly affects its solubility, crystallinity, and viscosity, as well as its optical properties [45]. Furthermore, the reactivity of chitosan depends on the available amino and hydroxyl groups. In particular, chitosan derivatives can be easily obtained by reacting chitosan primary amino groups as well as its primary or secondary hydroxyl groups [44]. Chitosan derivatives have been designed to improve specific properties of native chitosan, such as solubility [46]. Glycol-chitosan (G-chitosan), soluble at physiological pH, represents a paradigmatic example of a soluble chitosan derivative that has been widely exploited either for diagnostic [47] or therapeutic [48,49] applications in the nanomedical field. Chi-tosan biocompatibility and biodegradability were largely demonstrated [50]. Chitosan species and/or derivatives are also known to exert direct bacteriostatic or fungistatic ac-tivity against several microorganisms (including Staphylococcus spp., Streptococcus spp., and Candida spp.) [51]. Therefore, it has been widely exploited for the preparation of drug delivery systems for the treatment of chronic wounds, such as hydrogels, sponge-like dress-ings, films, and development of novel nanotherapeutics (nanoparticles, nanocomposites, and nanofibers) [52,53].
Based on these preconditions, the present work aimed at investigating and selecting the best candidate chitosan for OLND shell manufacturing in order to optimize OLND for-mulation parameters and stability. Here, four types of chitosan (i.e., LW, MW, G-, and MG-chitosan) were evaluated for the development of fine-tuned and well-characterized formu-lations in order to design a multivalent oxygen nanoreservoir for future potential treatment of chronic wounds in human patients. LW, MW, G-, and MG-cOLND nanoformulations were produced following a purposely tuned protocol as previously described [27] and were comparatively evaluated for physico-chemical properties, oxygen releasing abilities, and biocompatibility with human keratinocytes.
The chitosan shell was selected for its intrinsic properties and because it may be suitable for future drug loading, exploiting either chemical conjugation or electrostatic interactions with the functional groups of chitosan [54–56].
All chitosan-shelled OLNDs showed spherical morphology characterized by a well-defined core-shell structure. The presence of chitosan as an external coating can allow the oxygen release to be controlled and prolonged. All nanodroplets displayed average
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ters lower than 500 nm, except for MW cOLNDs. Specifically, LW cOLNDs showed the smallest average diameters with a value of about 400 nm. This result can be due to the pres-ence of a greater concentration of chitosan polymer at the external ND surface, compared to MW cOLNDs. In any case, all size values are suitable for skin application [57,58].
Zeta potential values ranging from +23 (G-cOLNDs) to +41 mV (MG- cOLNDs) were measured. Interestingly, cationic nanocarriers can be suitable for topical treatments as their positive charges interact strongly with the anionic surface of the skin, as demonstrated by Wu and colleagues [59] in a study showing that cationic fluorophore PMI-conjugated PS-NH3+amino functionalized polystyrene latex nanoparticles displayed brighter fluo-rescence at the skin surface than anionic PMI-conjugated PS-CO2-carboxyl-functionalised polystyrene nanoparticles.
Positive values of zeta potential showed the presence of chitosan on the OLND shell surfaces. Indeed, charged polysaccharides can be adsorbed by the phospholipid interfacial monolayer present at the ND interface, as previously shown [60,61]. Chitosan can interact with phospholipids mainly through electrostatic interactions, but also including H-bonding and hydrophobic forces [60,61]. The formation of a tight chitosan/DPPC monolayer on the OLND surface was confirmed by FTIR analysis. The different types of chitosan can markedly influence these interactions and affect the nanostructure at the interface. In addition, the presence of a charged shell can play a key role for system physical stability. Indeed, the surface charge is a crucial parameter to predict the stability of a nanocarrier, as it measures charge repulsion or attraction among particles. Taking into account a cationic polymer, zeta potential values higher than +20 mV are usually required for stability of colloid systems [62]. Interestingly, the cOLND zeta potential values are high enough to avoid ND aggregation phenomena. The physical stability of the formulations was confirmed by additional monitoring of cOLND physico-chemical parameters up to 6 months. G-cOLNDs appeared to be the least stable out of four formulations, showing a slight size increase over time. This result may be due to their lowest zeta potential value. On the contrary, LW cOLNDs displayed the highest stability because they did not show any size modification up to 6 months.
In addition, all the formulations showed a marked in vitro mucoadhesive activity. It is worth noting that chitosan is a mucoadhesive polymer. This property, due to the capability to establish ionic, hydrogen, and hydrophobic bonds with the negatively-charged mucin, was maintained in all the formulations. This feature can be exploited to enhance the residence time of cOLNDs in the wound area allowing an intimate contact between cOLNDs and skin lesions [63,64].
All the nanoformulations displayed similar oxygen storing capacity (~45 O2mg/L). The oxygen was slowly released from the internal core of the nanoformulations, delivering clinically relevant amounts of oxygen in a time-sustained manner by passive diffusion through the ND shell. This evidence confirmed cOLND suitability for topical treatment of chronic wounds, as normoxia-like phenotypes of hypoxic skin tissues might be restored due to the prolonged oxygen release. We can speculate that the OLNDs can be incorporated in a topical gel formulation for long-lasting oxygen release for wound care.
Clearly, OLND biocompatibility with human skin cells represents a crucial issue, since the potential use in vivo of oxygen nanocarriers might be compromised by their toxicity to eukaryotic cells. Interestingly, LW chitosan as such (especially chitosan with molecular weight <10000 Da) has been reported to be associated with lower toxicity and higher water solubility compared to chitosan molecules characterized by higher molecular weight [65]. Moreover, chitosan antimicrobial activity related to nanocarriers has been reported to depend on the molecular weight and degree of deacetylation of the chitosan employed during formulation manufacturing [66]. To assess OLND biocompatibility and to discern whether any cytotoxic effects might be related to a shell’s chitosan species or derivatives, LW, MW, G-, and MG-chitosan-shelled nanodroplets as well as free LW, MW, G-, and MG-chitosan aqueous solutions were incubated for 24 h with human keratinocytes. Interestingly, the production of keratinocyte matrix metalloproteinases, playing crucial
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roles during the remodeling phase of wound healing, was demonstrated to be altered by hypoxia. In addition, taking into account that the donor’s age is a key factor [67], the human keratinocyte cell line employed here (HaCaT cell line) was immortalized from a 62-year-old donor, therefore fitting as a reasonable in vitro model for our studies. Biocompatibility was checked through three different yet complementary assays, measuring cell viability, treatment toxicity, and cell metabolic activity. Results from all three studies were consistent, showing that LW, MW, or G-chitosan (either free or as nanodroplet coating) were highly compatible with viability, health, and metabolism of human keratinocytes, whereas MG-chitosan was not.
The higher cytotoxicity of MG-cOLNDs can be ascribed to the presence of quaternary ammonium groups belonging to MG-chitosan that are protonated at any pH values.
Further analyses by confocal microscopy were also carried out to discern the mech-anisms of interaction between cOLNDs and human cell surfaces (i.e., lack of contact, adhesion, or internalization). According to the obtained results, all nanodroplet formu-lations were avidly uptaken by HaCaT cells after 24 h of incubation. This evidence is in line with previous results obtained with dextran OLNBs in monkey fibroblastoid kid-ney cells [25], with dextran OLNDs in human endothelial cells [30], keratinocytes [28], and monocytes [31], and with MW cOLNDs in human keratinocytes [37] and breast cancer cells [38]. Additionally, the internalization of chitosan/cyclodextrin nanoparticles by ep-ithelial cells [68] have been reported. Further studies aimed at clarifying the mechanisms underlying the physical interaction between cOLNDs and human keratinocytes will be performed. Nevertheless, it is legitimate to speculate that after interacting with human cells, nanoparticles might be engulfed in invaginations of the cell membrane and then be internalized by cells through time-, concentration-, and energy-dependent pinocytic processes [69]. Macropinocytosis, clathrin-mediated endocytosis, caveolae-mediated endo-cytosis, and mechanisms independent of clathrin and caveolin are examples of these uptake mechanisms [70,71]. These processes can activate several intracellular signaling pathways, thus paving the way for different cellular fates, from proliferation and survival to apoptosis and cell death [72,73]. Chitosan intracellular degradation has been suggested to be associ-ated with lysosomes [74]. Specific receptors for chitosan have not been reported to date, suggesting that the mechanism of chitosan’s cellular binding might be a nonspecific electro-static interaction with the negatively charged cell membrane. Interestingly, keratinocytes have been reported to expose several anionic residues on their membranes, supporting the present data on chitosan-shelled OLND cellular internalization after adhering on cell plasma membrane. Future studies aiming at elucidating the processes underlying cellular internalization and trafficking of nanodroplets will be considered.
4. Materials and Methods
4.1. Materials and Instruments
Sterile plastics were from Costar (Corning, NY, USA), Jet Biofil (Guangzhou, China), and VWR (Radnor, PA, USA); ethanol (96%) was provided by Carlo Erba (Milan, Italy); soybean lecithin (Epikuron 200®) was from Cargill (Hamburg, Germany); the 1–800 Mil-lipore system to obtain ultrapure water was from MilMil-lipore (Molsheim, France); Ultra-Turrax SG215 homogenizer was from IKA (Staufen, Germany); the optical microscope XDS-3FL Optika from Ponteramica, Italy; the Philips CM10 electron microscope was from Philips (Eindhoven, Netherlands); the Nanobrook 90Plus Particle Size Analyzer was from Brookhaven (New York City, NY, USA); the Hach Lange LDO oximeter was from Hach Lange (Derio, Spain); the Beckman Coulter Allegra 64R Centrifuge was from Beckman Coulter (Brea, CA, USA); the Orion Model 420A pH Meter was from Thermo Scientific (Waltham, MA, USA); the HaCaT cells were from Cell Line Service GmbH (Eppelheim, Ger-many); Dulbecco’s Modified Eagle Medium (DMEM) and RPMI 1640 medium were from Invitrogen (Carlsbad, CA, USA); streptomycin was from Cambrex Bio Science (Vervies, Bel-gium); the humidified CO2/air-incubator was from Thermo Fisher Scientific Inc. (Waltham, MA, USA); the LSM710 inverted confocal laser scanning microscope equipped with
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Neofluar 63×1.4 oil objective was from Zeiss (Oberkochen, Germany); the Synergy HT microplate reader was from Bio-Tek Instruments (Winooski, VT, USA; the CellTiter-Glo® Kit was from Promega (Madison, WI, USA); Prism version 8.0 software was from Graph-Pad Software (San Diego, CA, USA). 1,1,1,2,3,4,4,5,5,5-Decafluoropentane (purity ~60%), chitosan low molecular weight (degree of deacetylation 75–85%, 50–190KDa), chitosan medium molecular weight (degree of deacetylation 75–85%, 190–310 KDa), glycol chitosan (degree of polymerization≥400, purity≥60%), and methyl glycol chitosan (≥70%) were obtained from Sigma–Aldrich (St. Louis, MO, USA). Any additional materials that are not listed here were from Sigma–Aldrich, St. Louis, MO, USA.
4.2. Development and Manufacturing of Formulations 4.2.1. Preparation of OLND and Control Formulations
OLNDs were prepared following a multi-step protocol that was previously designed, patented, and described by the present research group [27]. Briefly, 300 µL of an ethanol solution containing Epikuron®200 and palmitic acid (1% w/v) were added to 500 µL of DFP under magnetic stirring to obtain a pre-emulsion. Then, 4.8 mL of ultrapure water was added, and the system was homogenized using an Ultra-Turrax SG215 homogenizer for 2 min at 24,000 rpm. Thereafter, the sample was saturated with O2for 10 min. Finally, to obtain the polymeric NDs, 300 µL of LW, MW, G-, or MG-chitosan aqueous solution (1% w/v, pH 5.0) was added drop-wise under magnetic stirring. Control formulations (free MW, LW, G-, or MG-chitosan solutions, OFND suspensions, and oxygen-saturated solution (OSS)) were prepared by following shortened versions of the above-described protocol: Briefly, free chitosan solutions were obtained through proper dilution of MW, LW, G-, or MG-chitosan (1% w/v) in order to reach chitosan concentrations that were equivalent to those contained in ND formulations, whereas OFND formulations were obtained by omitting during ND manufacturing protocol the addition of O2. For biological experiments, all formulations were prepared in phosphate buffer saline (PBS) pH 7.4 instead of ultrapure water. For confocal microscopy experiments, fluorescent NDs were obtained by adding 6-coumarin (1 mg/mL) to the DFP core.
4.2.2. Sterilization of the Formulations
Firstly, the sterilization of the glassware and the components was carried out at 121◦C and at a pressure of 2 bar. Subsequently, the formulations were sterilized by exposure to UV-C for 20 min. At the end, UV-C-treated materials were incubated with cell culture RPMI 1640 medium in a humidified CO2/air-incubator at 37◦C for up to 72 h, in order to check any microbial contamination via optical microscopy.
4.3. Characterisation of Formulations
4.3.1. Characterization of ND Formulations
The average diameter, polydispersity index, and zeta potential of cOLNDs were acquired by dynamic laser scattering (DLS). The measurements were carried out using a particle size analyzer at a scattering angle of 90◦ and at 25◦C. ND nanosuspensions were diluted in deionized filtered water before the analyses. The determination of the zeta potential was obtained by placing the diluted ND formulations in the electrophoretic cell, in which a 15-V/cm electric field was applied. The morphology of formulations was observed by transmission electron microscopy (TEM). ND aqueous suspensions were sprayed on a Formwar-coated copper grid and air-dried before analysis. The osmolarity of the ND formulations was determined at 25◦C using a Knauer osmometer, whereas their viscosity was determined at 25◦C using a Ubbelohde capillary viscosimeter (Schott Gerate, Mainz, Germany).
Fourier transformed infrared (FTIR) analysis was performed using a Perkin Elmer Spectrum 100 FT-IR (Perkin Elmer, Branford, CT, USA). The FTIR spectra of the samples were collected in the region 4000−1–650−1. Data acquisition was carried out using spectrum software version 10.03.05 Perkin Elmer Corporation.
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A DSC/7 differential scanning calorimeter (Perkin–Elmer, Branford, CT, USA) equipped with a TAC 7/DX instrument controller and the Pyris program were used for thermal analysis. Before performing the analyses, the instrument was calibrated with indium for melting point and heat of fusion. A heating rate of 10◦C/min was set in the 25–200◦C range. Analyses were carried out in triplicate on about 20 mg of sample aqueous suspen-sion placed in standard aluminum sample pans for liquids (Perkin–Elmer) under nitrogen purge. An empty aluminum pan was used as the reference standard.
4.3.2. OLND and OSS Oxygen Content
The oxygen content of OLNDs and OSS was determined by adding known amounts of sodium sulphite and measuring the generated sodium sulphate, according to Reaction (1):
Na2SO3+ 1
2 O2→Na2SO4 (1)
The amount of sodium sulphate was estimated by gravimetric method after the addition of barium chloride. Briefly, an excess of barium chloride was added to the sample under stirring. The formed precipitate was collected on a filter, washed, and, after drying, was weighted.
4.3.3. ND Stability over Time
The physical stability of NDs was investigated by morphological analysis and by size and surface charge determination over time for up to six months. ND morphology was observed by TEM to confirm the integrity of ND structure.
4.3.4. Mucoadhesion Test
The in vitro mucin adhesion assay was selected to evaluate the ND mucoadhesive properties. For this purpose, the mucin and ND interaction was determined by turbidi-metric analysis. The ND nanosuspensions were mixed with a mucin solution (1 mg/mL) at a 1:1 (v/v) ratio and left under magnetic stirring for 30 min. Then, the sample was centrifuged for 5 min at 20,000 rpm and the transmittance of the supernatant was measured at 500 nm with an UV spectrophotometer (Du730 spectrophotometer, Beckman, Coulter, Fullerton, CA, USA) to determine the amount of free mucin. The concentration of mucin was calculated using an external standard method. A calibration curve in the concen-tration range between 0.1 to 1 mg/mL was obtained by analyzing the transmittance of aqueous stock standard solutions. The amount of mucin bound to NDs was determined by subtracting the free mucin content in the supernatant from the total amount of mucin. 4.4. In Vitro Oxygen Release
The in vitro oxygen release was evaluated by a dialysis method. The cOLND formu-lations were sealed in a dialysis bag (cut-off 12,000–14,000 Da) immersed in the hypoxic receiving phase (NaCl 0.9% w/v solution with an oxygen concentration reduced up to 1 mg/L by a N2purge). The concentration of oxygen released from the different cOLND formulations and OSS into the hypoxic solution was measured up to 24 h through Hach Lange LDO oximeter, displaying an accuracy of 0.01 mg/L. Before each measurement, the oximeter was calibrated in air, until stable temperature and humidity conditions were reached.
4.5. Human Biocompatibility Studies 4.5.1. Human Keratinocyte Cell Cultures
For the studies presented here we used the HaCaT, a spontaneously transformed line of adult human skin keratinocytes from a 62-year-old Caucasian male donor [75]. Cells, used for the assessment of chitosan and ND biocompatibility, were grown as adherent monolayers in DMEM supplemented with 10% fetal bovine serum, 100 U/mL penicillin, 100 µg/mL streptomycin, and 2 mM/L glutamine at 37◦C in a humidified atmosphere
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containing 5% CO2. Before starting the experiments, cells were washed with PBS1x, detached with trypsin/ethylenediaminetetraacetic acid (0.05/0.02% v/v), resuspended, and plated with fresh DMEM at standard cell densities, as detailed in the following sections. 4.5.2. ND Internalization by Human Keratinocytes
Confocal microscopy was used to evaluate the ND internalization by human ker-atinocytes. HaCaT cells (6×104cells/mL in 24-well plates) were divided into untreated or treated with 10% v/v 6-coumarin-labeled MW, LW, G-, or MG-chitosan-shelled OLND or OFND nanosuspensions for 24 hours under normoxic condition (20% O2) in a humidified CO2/air-incubator at 37◦C. Then, HaCaT were fixed with 1% paraformaldehyde solution for 15 min at RT and were incubated with 15 µg/mL propidium iodide (PI) to visualize nucleic acids. Confocal images were acquired by using an Olympus IX70 inverted laser scanning confocal microscope, and captured using FluoView 200 software (Olympus Amer-ica Inc., Melville, NY, USA). Wavelengths of 488 and 568 nm were used to detect NDs or the labeled nuclei, respectively. The acquisition time was 400 ms.
4.5.3. Human Keratinocyte Cell Viability
Cell viability was evaluated using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. HaCaT cells (105cells/mL in 96-well plates) were left untreated or treated with 10% v/v MW, LW, G-, or MG-chitosan free solution or chitosan-shelled OLND/OFND nanosuspensions. After incubation for 24 h under 5% CO2 at 37 ◦C, the medium was discarded and 20 µL of MTT in PBS (5 mg/mL) were added to the cells for 3 additional hours at 37◦C. After plate centrifugation and cell supernatant dis-carding, the dark blue formazan crystals were dissolved using 100 µL of sodium dodecyl sulphate (SDS). The absorbance of the resulting solutions was measured at 550 nm using a Synergy HT microplate reader at a reference wavelength of 650 nm. Data were expressed as percentage of viability.
4.5.4. Chitosan and ND Cytotoxicity on Human Keratinocytes
The potential cytotoxic effects of free chitosan solutions and chitosan-shelled ND suspensions were quantitated measuring lactate dehydrogenase (LDH) release from the cells into the extracellular medium. HaCaT cells (1.5× 105 cells/mL in 6-well plates) were left untreated or treated with 10% v/v MW, LW, G-, or MG-chitosan solutions or chitosan-shelled OLND/OFND nanosuspensions for 24 hours under normoxic condition at 37◦C. Then, the culture supernatant (1 mL) was harvested and centrifuged at 13,000×g for 30 min. Cells were washed with fresh medium, detached with scraper, washed with PBS 1×, resuspended in 1 mL of 82.3 mM triethanolamine solution, pH 7.6 (TRAP), and son-icated on ice with a 10 s burst. Then, 5 µL of cell lysates and 50 µL of cell supernatants were diluted with TRAP supplemented with 0.5 mM sodium pyruvate and 0.25 mM nicoti-namide adenine dinucleotide reduced form (NADH). The Synergy HT microplate reader was used to monitor the reaction, measuring absorbance at 340 nm (37◦C). The intracel-lular and extracelintracel-lular LDH activities, expressed as µmol of oxidized NADH/min/well, was determined and the cytotoxicity was eventually calculated as the net ratio between extracellular and total (intracellular + extracellular) LDH activities.
4.5.5. ATP Production by Human Keratinocytes
The number of metabolically active cells in culture was evaluated by determining the levels of adenosine triphosphate (ATP) secreted by the cells into the culture medium. HaCaT cells (6 × 104 cells/mL in 24-well plates) were left untreated or treated with 10% v/v MW, LW, G-, or MG-chitosan solutions or cOLND/cOFND nanosuspensions for 24 h in a humidified CO2/air-incubator at 37◦C. Then, cell supernatants were collected and ATP levels were measured by using the CellTiter-Glo® Luminescent Cell Viability Assay Kit, following the manufacturer’s instructions [76].
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4.6. Statistical Analysis
At least three independent experiments, each one in duplicate or triplicate, were per-formed for every investigational study. Results are shown as means±SD for descriptive results or as means±SEM for inferential results. Imaging data are shown as representative pictures. Numerical data were also analyzed for significance by a two-way analysis of variance (ANOVA) followed by Tukey’s post-hoc test through GraphPad Prism 8 software (GraphPad, San Diego, CA, USA), with p < 0.05 being considered as significant.
5. Conclusions
In the present study, four different types of chitosan (LW, MW, G-, and MG-chitosan) were challenged as candidate biopolymers for OLND shell manufacturing. The aim of the work was to develop fine-tuned and well-characterized OLNDs, in order to identify an optimized formulation for topical application in wound healing. cOLNDs were analyzed for their physico-chemical characteristics, oxygen releasing abilities, and biocompatibility as well as interaction with human keratinocytes. All chitosan-shelled nanodroplets displayed spherical morphology, cationic surfaces, and diameters in the nanometer range, with LW cOLNDs being the smallest one. They showed mucoadhesive properties and the capability to store and release oxygen in a sustained manner. After cellular internalization, MG-cOLNDs proved to be highly toxic to human keratinocytes, whereas all other OLND formulations were well tolerated. Based on these findings, LW chitosan appears to be the best candidate biopolymer for OLND shell manufacturing, as it associates with the smallest sizes, the highest stability, and the lowest toxicity of nanodroplets. For these reasons, LW chitosan should be employed as the polysaccharide of choice in any future studies aimed at testing the effectiveness of cOLNDs as potential skin devices to treat chronic wounds.
Author Contributions:Conceptualization, M.P., G.B., N.M., and R.C.; methodology, M.A., A.L., T.G., and A.T.; formal analysis and investigation, M.A., B.B., A.L., N.F., and T.G.; data curation, M.P., R.C., M.A., G.B., and N.M.; writing—original draft preparation, M.P. and M.A.; writing—review and editing, R.C. and G.G.; supervision, R.C., A.M.C., and and G.G. All authors have read and agreed to the published version of the manuscript.
Funding:The present work was supported by funds from Fondazione Cariplo (HyWonNa project, grant no. 2015-0550 to MP), University of Torino (ex 60% to RC, MA), Fondazione CRT (CRT 2018, grant no. 2018.AI991.U1128 to NM) and Compagnia di San Paolo (Torino_call2014_L2_207 to AMC). Institutional Review Board Statement:Not applicable.
Acknowledgments: The authors would like to thank Francesca Pecoraro and Stefano Turini for helping with cellular studies, Giorgio Gribaudo for allowing us to use his lab facilities to perform confocal microscopy studies, and Caterina Guiot, Nicoletta Basilico, and Mario Dell’Agli for their comments on the study.
Conflicts of Interest:The authors declare no conflict of interest. References
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